Autosomal dominant hereditary disorder	Congenital hamartoma	Congenital melanosis	Digestive system hereditary disorder	Disorder of digestive system specific to fetus OR newborn	Hamartoma of intestine	Hereditary cancer-predisposing syndrome	Hereditary disorder of nervous system	Hereditary disorder of the integument	Intestinal polyposis syndrome	Lentiginosis	Neurocutaneous syndrome
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Peutz-Jeghers syndrome (disorder)
	Peutz-Jeghers syndrome
	PJS - Peutz-Jeghers syndrome Periorificial lentiginosis syndrome Peutz-Jeghers polyposis Perioral lentiginosis

Id	54411001
Status	Defined

Associated morphology	Neoplasm
Finding site	Structure of nervous system
Occurrence	Congenital

Associated morphology	Peutz Jeghers polyp
Finding site	Intestinal structure
Occurrence	Congenital

Associated morphology	Neoplasm
Finding site	Skin structure
Occurrence	Congenital

Associated morphology	Lentigo
Finding site	Structure of skin and/or mucous membrane
Occurrence	Congenital

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q85.8
Term	Overige gespecificeerde facomatosen, niet elders geclassificeerd

SNOMED CT to ICD-10 extended map

Target	Q85.8
Rule	TRUE
Advice	ALWAYS Q85.8
Correlation	SNOMED CT source code to target map code correlation not specified

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Peutz-Jeghers polyps of small bowel